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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14302생성일: 2026년 10월 24일

Oxazole → Methyl 3-{[ethyl(propyl)amino]carbonyl}-5-(1,3-oxazol-2-yl)benzoate

https://huagongshe.com/ko/reaction/14302

반응식

참여 물질

역할이름HCID투입량
반응물OxazoleHCID 9255—
반응물Methyl 3-{[ethyl(propyl)amino]carbonyl}-5-iodobenzoateHCID 21086183—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Methyl 3-{[ethyl(propyl)amino]carbonyl}-5-(1,3-oxazol-2-yl)benzoateHCID 21086182—

반응 조건

온도0 °C

반응 단계

To a −70° C. stirred solution of oxazole (106 mg, 1.5 mmol) in tetrahydrofuran (4 mL) is added n-butyllithium (1.6 M in hexanes, 1.0 mL, 1.7 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 4.6 mL, 4.6 mmol) is added and the reaction mixture is warmed to 0° C. for 1 h. To this mixture is added a solution of methyl 3-{[ethyl(propyl)amino]carbonyl}-5-iodobenzoate (535 mg, 1.45 mmol) in anhydrous tetrahydrofuran (1.8 mL) followed by palladium(0)tetrakis(triphenylphosphine) (120 mg, 0.10 mmol). The reaction mixture is heated at reflux for 2 h. The reaction mixture is cooled, diluted with ethyl acetate, washed with water, and saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 60% ethyl acetate/hexane) provides the title compound. ESI MS m/z 317.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-99f179976a1448d08a0d2b74a72f991c
출처 메모uspto-grants-2010_06